Реакция #1884980

ord-33d43e2ca56e4085aa6fc548719e417b

Уравнение реакции

C=CCCCSC(C)(C)[C@H](NC(=O)OC(C)(C)C)C(=O)OC
N-tert-butoxycarbonyl-3-(4-pentenylthio)-L-valine, methyl ester
O.[Li+].[OH-]
lithium hydroxide monohydrate
Cl
hydrochloric acid
C=CCCCSC(C)(C)[C@H](NC(=O)OC(C)(C)C)C(=O)O
N-tert-butoxycarbonyl-3-(4-pentenylthio)-L-valine
Выход 99.3%

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Промывкаwashed with water (3×) and brine
  2. 2
    Сушкаdried over anhydrous sodium sulfate
  3. 3
    Фильтрацияfiltered
  4. 4
    Концентрированиеconcentrated under vacuum

Методика

To a solution of 8.52 g (25.7 mmol) of N-tert-butoxycarbonyl-3-(4-pentenylthio)-L-valine, methyl ester in 200 mL of tetrahydrofuran at room temperature was added a solution of 1. Og (26.2 mmol) of lithium hydroxide monohydrate in 50 mL of water. The resulting mixture was stirred at room temperature for 65 hours. To the reaction mixture then was added 28 mL of 1.00N hydrochloric acid. The mixture was diluted with diethyl ether, washed with water (3×) and brine, dried over anhydrous sodium sulfate, filtered, and concentrated under vacuum to afford 8.10 g of N-tert-butoxycarbonyl-3-(4-pentenylthio)-L-valine as a colorless oil. NMR (300 MHz, CDCl3): δ 5.75 (d of d of t, 1 H, J=17.2, 10.3, 6.6 Hz), 5.40 (br s, 1 H), 5.05-4.94 (m, 2 H), 4.28 (br s, 1 H), 2.56 (m, 2 H), 2.13 (quart., 2 H, J=7.3 Hz), 1.63 (quint., 2 H, J=7.3 Hz), 1.44 (s, 9 H), 1.39 (s, 3 H), 1.37 (s, 3 H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08343477B2uspto-grants-2013_01